Determinants of intracranial microcalcification assessed by 18F-sodium fluoride PET.
Authors
Affiliations (5)
Affiliations (5)
- Department of Radiology, University of Pennsylvania.
- Sidney Kimmel Medical College, Thomas Jefferson University.
- Drexel University College of Medicine, Philadelphia, Pennsylvania, USA.
- Department of Nuclear Medicine, Odense University Hospital.
- Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
Abstract
Intracranial calcifications are commonly found in adults and may represent either benign or pathological lesions. Conventional imaging modalities detect static macrocalcifications but do not capture molecular microcalcification. In this study, we used 18F-sodium fluoride (NaF) PET/computed tomography (CT) to idetect intracranial molecular microcalcification. A total of 127 subjects underwent 18F-NaF PET/CT 90 min following radiotracer injection. Artificial intelligence-based quantification was performed to obtain regions of interest for the brainstem, basal ganglia (caudate and lentiform nuclei), insula, thalamus, and ventricles. Linear regression models were used to correlate NaF mean standardized uptake value (SUVmean) with various clinical factors. NaF SUVmean was highest in the insula (0.8 ± 0.4) and brainstem (0.8 ± 0.3), while uptake was lowest in the caudate nucleus (0.1 ± 0.1). No differences were found in NaF SUVmean between healthy volunteers and at-risk patients. On multivariate regression, NaF SUVmean directly correlated with age in the brainstem (β = 0.01, P = 0.01), lentiform nucleus (β < 0.01, P = 0.02), and ventricles (β < 0.01, P < 0.01). Male sex inversely correlated with NaF SUVmean in the insula (β = -0.30, P < 0.01). There was an association between NaF SUVmean and BMI in the brainstem, caudate nucleus, lentiform nucleus, thalamus, and ventricles (β ≤ 0.01, P < 0.01 in all regions). Thalamic and ventricular NaF SUVmean directly correlated with hypertension on univariate but not multivariate analysis. NaF PET/CT detects intracranial molecular microcalcification that is not visible on conventional CT and may provide insight into pathology associated with this biological process.